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Katalógové číslo: (APOSBIA4401-2.5KG)
Dodávateľ: Apollo Scientific
Opis: 1-O-Acetyl-2,3,5-tri-O-benzoyl-beta-D-ribofuranose 2.5kg pack 1 * 2,5 kg
Merná jednotka: 1 * 2,5 kg

New Product


Dodávateľ: METTLER TOLEDO
Opis: Modular triple-channel instruments with touch screen operation, which can easily handle the most complex applications and meet stringent requirements in regulated markets.

Dodávateľ: METTLER TOLEDO
Opis: Not only do these meters measure pH and ORP with classical sensors, but they also support pH measurement with ISFET technology. The instruments can effectively cope with complex applications and stringent requirements in regulated markets as well as with routine measurement tasks in laboratories.

Dodávateľ: METTLER TOLEDO
Opis: This single-channel instrument can easily handle the most complex applications and meets stringent requirements in regulated markets. The meter is flexible and can be modularly expanded with additional measurement parameters at any time. Special methods for the most common incremental ion measurement techniques are included, such as standard addition, subtraction and sample addition and subtraction methods.
Katalógové číslo: (ABCAAB284623-1X96)
Dodávateľ: ABCAM
Opis: Human SEMA4C ELISA Kit is a single-wash 90-min Simplestep used to quantify Human SEMA4C with a sensitivity of 23,5 pg/ml. The assay uses a simple mix-wash-read protocol with just one incubation and one wash step. - Colorimetric Sandwich ELISA - 450 nm readout : works on any standard plate reader.
Merná jednotka: 1 * 96 Tests


Katalógové číslo: (ABCAAB284619-1X96)
Dodávateľ: ABCAM
Opis: Rat Kallikrein 10 ELISA kit is a single-wash 90-min Simplestep used to quantify Rat Kallikrein 10 with a sensitivity of 2,35 pg/ml. The assay uses a simple mix-wash-read protocol with just one incubation and one wash step. Colorimetric Sandwich ELISA - 450 nm readout: works on any standard plate reader.
Merná jednotka: 1 * 96 Tests


Dodávateľ: ABCAM
Opis: Mouse Erythropoietin ELISA kit (EPO) is a single-wash 90-min Simplestep used to quantify Mouse Erythropoietin (EPO) with a sensitivity of 2.35 pg/ml. The assay uses a simple mix-wash-read protocol with just one incubation and one wash step. Colorimetric Sandwich ELISA - 450 nm readout: works on any standard plate reader - Different formats for different needs: 10×96 plates for bulk orders.

Dodávateľ: METTLER TOLEDO
Opis: These instruments with two or three channels are modularly expandable with additional measurement parameters at any time.

Dodávateľ: MP BIOMEDICALS
Opis: Glutaraldehyde is also referred to as glutaral, 1,5-pentanedione, potentiated acid glutaraldehyde, sonacide, and glutardialdehyde. Pure monomeric glutaraldehyde has an absorbance peak at 280 nm and the main impurity, possibly a polymer, has an absorbance peak at 235 nm. Upon analysis, this product is 25-28% by titration and has an A235/A280 ratio of not more than 0,5. Monomeric glutaraldehyde may be purified from polymeric glutaraldehyde by treatment with charcoal (5% w/v) and subsequent filtration (3-4 times). Untreated glutaraldehyde has an absorption at 235 nm that is 5 times greater than that at 280 nm, whereas, after three washings the values are about equal. Glutaraldehyde is a bifunctional cross-linking reagent, reacting with NH2 groups to form Schiff's bases.

Katalógové číslo: (ABCAAB210580-96)
Dodávateľ: ABCAM
Opis: Mouse PRAS40 ELISA kit is a single-wash 90-min Simplestep used to quantify Mouse PRAS40 with a sensitivity of 23,5 pg/ml. The assay uses a simple mix-wash-read protocol with just one incubation and one wash step. - Colorimetric sandwich ELISA - 450 nm readout : works on any standard plate reader - Design your own immunoassay: we also offer the conjugation-ready antibody pair.
Merná jednotka: 1 * 96 Tests


Katalógové číslo: (BOSSBS-13623R-CY7)
Dodávateľ: BIOSS INC
Opis: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-13623R-A555)
Dodávateľ: BIOSS INC
Opis: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-13623R-A350)
Dodávateľ: BIOSS INC
Opis: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-13623R)
Dodávateľ: BIOSS INC
Opis: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-13623R-CY5)
Dodávateľ: BIOSS INC
Opis: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
Merná jednotka: 1 * 100 µl


Katalógové číslo: (BOSSBS-13623R-CY3)
Dodávateľ: BIOSS INC
Opis: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
Merná jednotka: 1 * 100 µl


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Zásoby tejto položky sú obmedzené, no môžu sa nachádzať v inom sklade blízko pri vás. Uistite sa prosím, že ste prihlásený/á na tejto lokalite, aby sa mohli zobraziť dostupné zásoby. Ak sa stále zobrazuje zavolajte a potrebujete pomoc, zavolajte nám prosím na číslo +43 1 97002 - 0.
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